A Novel APOC2 Mutation in a Colombian Patient with Recurrent Hypertriglyceridemic Pancreatitis

Hypertriglyceridemia is a common disease with only 2% of cases exhibiting monogenic mutations. Familial chylomicronemia syndrome (FCS) is a rare genetic condition associated with recurrent and severe episodes of pancreatitis and is mainly caused by mutations in the LPL gene, with few cases related t...

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Detalles Bibliográficos
Autores principales: Pinilla-Monsalve, Gabriel D, Lores, Juliana, Pachajoa, Harry, López-Ponce de León, Juan D, López, Alejandro, Rodríguez-Rojas, Lisa X, Nastasi-Catanese, José A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125404/
https://www.ncbi.nlm.nih.gov/pubmed/32280258
http://dx.doi.org/10.2147/TACG.S243148

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125404/
https://www.ncbi.nlm.nih.gov/pubmed/32280258
http://dx.doi.org/10.2147/TACG.S243148

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